FDA Device recall Z-1710-2020
Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer
- FDA Device
- Class II
- ongoing
- Published 2020-05-06
On 2020-05-06 the FDA classified a Class II recall of Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer by Ge Healthcare, citing an issue with the Lunar iDXA control panel may cause the start button to not release and potentially contribute to an accidental radiation occurrence.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1710-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-12-03 |
| Published | 2020-05-06 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer
Reason
An issue with the Lunar iDXA control panel may cause the start button to not release and potentially contribute to an accidental radiation occurrence.
Identifiers
| code_info | all affected systems |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1710-2020%22
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